Disinfecting caps having sealing features and related systems and methods

ABSTRACT

Caps can be used to cover and disinfect medical connectors. Some caps can create a seal with the medical connectors to prevent antiseptic from entering a fluid paths defined by a connector. Support members can aid in creating or maintaining the seal.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of U.S. Provisional PatentApplication No. 61/265,216, titled STERILIZATION CAPS AND SYSTEMS ANDASSOCIATED METHODS, filed Nov. 30, 2009; and this application is acontinuation-in-part of U.S. patent application Ser. No. 12/917,336,titled DISINFECTING CAPS AND SYSTEMS AND ASSOCIATED METHODS, filedNovember 1, 2010, which is a continuation-in-part of U.S. patentapplication Ser. No. 12/610,141, titled STERILIZATION CAPS AND SYSTEMSAND ASSOCIATED METHODS, filed Oct. 30, 2009, the entire contents of eachof which are hereby incorporated by reference herein. The earliest dateto which this application claims priority is Oct. 30, 2009.

BACKGROUND

1. Technical Field

The present disclosure generally relates to caps for medical connectorsand more specifically relates to caps that can be used to protect thecleanliness of unconnected medical connectors, such as connectors thatmay be used for fluid flow or for fluid delivery systems. Someembodiments are directed to caps for medical connectors that includemale-type interfaces and/or medical connectors that include female-typeinterfaces.

2. Related Art

Bloodstream infections, such as may be caused by microorganisms thatenter patients via intravascular catheters, are a significant cause ofillness and excess medical costs. A substantial number of suchinfections occur in U.S. intensive care units annually. Additionally, asignificant fraction of these infections result in death.

Guidelines from the Centers for Disease Control and Prevention describevarious ways to limit bloodstream infections in hospital, outpatient,and home care settings. The guidelines address issues such as handhygiene, catheter site care, and admixture preparation. However, despitethese guidelines, such infections continue to plague healthcare systemsat relatively unchanged rates.

Impregnating catheters with various antimicrobial agents is one approachfor reducing these infections. Impregnated catheters, however, provideless than satisfactory results. Additionally, some microbes havedeveloped resistance to the various antimicrobial agents used in thecatheters. Other systems and approaches have also been developed, butthese likewise suffer from a variety of limitations and drawbacks.

BRIEF DESCRIPTION OF THE DRAWINGS

The written disclosure herein describes illustrative embodiments thatare non-limiting and non-exhaustive. Reference is made to certain ofsuch illustrative embodiments that are depicted in the figures, inwhich:

FIG. 1 is a perspective view of an embodiment of an assembly thatincludes an embodiment of a female cap and an embodiment of a male cap,which can be connected in a pre-use configuration via a sleeve;

FIG. 2 is an exploded perspective view of the assembly of FIG. 1;

FIG. 3 is a perspective view of an embodiment of a sleeve that iscompatible with the assembly of FIG. 1;

FIG. 4A is a top plan view of an embodiment of a housing portion of afemale cap that is compatible with the assembly of FIG. 1;

FIG. 4B is a side elevation view of the housing portion of the femalecap of FIG. 4A;

FIG. 4C is a front elevation view of the housing portion of the femalecap of FIG. 4A;

FIG. 5A is a top plan view of an embodiment of a housing portion of amale cap that is compatible with the assembly of FIG. 1;

FIG. 5B is a side elevation view of the housing portion of the male capof FIG. 5A;

FIG. 5C is a front elevation view of the housing portion of the male capof FIG. 5A;

FIG. 6 is a cross-sectional view of the assembly of FIG. 1 taken alongthe view line 6-6 in FIG. 1;

FIG. 7A is a top plan view of the assembly of FIG. 1;

FIG. 7B is a top plan view of the assembly of FIG. 1 showing a male capportion thereof having been rotated so as to assist in the release ofthe male cap from the assembly;

FIGS. 8A-8D are cross-sectional views that depict various stages of anillustrative method for coupling a medical connector with the male capof FIGS. 1 and 6;

FIG. 9 is a perspective view of an embodiment of a medical connectorwith which various embodiments of caps can be used;

FIGS. 10A-10C are cross-sectional views that depict various stages of anillustrative method for coupling the medical connector of FIG. 9 withthe female cap of FIGS. 1 and 6;

FIG. 11 is a side elevation view of another embodiment of an assemblythat includes an embodiment of a female cap and an embodiment of a malecap, which can be connected in a pre-use configuration via a sleeve;

FIG. 12 is a perspective view of the female cap of FIG. 11;

FIG. 13 is a perspective view of an embodiment of a sealing member thatis compatible with the female cap of FIG. 11;

FIG. 14 is a cross-sectional view of the cap of FIG. 11 coupled with amedical connector;

FIG. 15 is an enlarged cross-sectional view of the cap of FIG. 11coupled with the medical connector that is taken along the view line15-15 in FIG. 14;

FIG. 16 is a side elevation view of another embodiment of a cap that isconfigured to form a seal with a medical connector;

FIG. 17 is a top plan view of the cap of FIG. 16;

FIG. 18 is a cross-sectional view of the cap of FIG. 16;

FIG. 19A is a cross-sectional view of the cap of FIG. 16 illustrating aninitial stage of coupling the cap with a medical connector;

FIG. 19B is a cross-sectional view of the cap of FIG. 16 illustrating afinal stage of coupling the cap with a medical connector;

FIG. 20 is a partial cross-sectional perspective view of anotherembodiment of a cap that is configured to form a seal with a medicalconnector;

FIG. 21 is a partial cross-sectional perspective view of anotherembodiment of a cap that is configured to form a seal with a medicalconnector;

FIG. 22 is a partial cross-sectional perspective view of anotherembodiment of a cap that is configured to form a seal with a medicalconnector;

FIGS. 23A-23C are cross-sectional views illustrating various stages ofcoupling another embodiment of a cap with a medical connector;

FIG. 24 is a side elevation view of another embodiment of a cap that isconfigured to form a seal with a medical connector; and

FIG. 25 is a perspective view of a fluid line that includes a coupledset of connectors that are amenable to being coupled with male andfemale caps, respectively.

DETAILED DESCRIPTION

Disclosed herein are disinfecting caps, and related systems and methods,that can protect and/or disinfect medical connectors. The caps, systems,and methods can reduce the threat of microorganisms entering thebloodstream of a patient via fluid flow or fluid delivery systems, suchas, for example, stopcocks, female luer lock connectors, or otherconnectors having female-type interfaces. The disinfecting caps can beincluded in systems or assemblies that include additional caps (e.g.,male caps), which may be used with connectors having male-typeinterfaces, such as fluid transfer devices having an elongated maleportion or male protrusion. For example, the caps may be configured foruse with a male luer connector. In some embodiments, a cap can beconfigured to couple with and disinfect a medical connector having anopen conduit or lumen, which may be shaped substantiallyfrustoconically, cylindrically, or in any other suitable shape. Thefemale cap can include a sealing member that is configured to plug orseal the open conduit. In further embodiments, the cap can include anantiseptic, and can be configured to dispense the antiseptic after theopen conduit has been sealed so as prevent antiseptic from entering theconduit, or more generally, from entering a fluid line. In someembodiments, the antiseptic may be contained within a pad prior to thecoupling of the cap to the medical connector, and the act of couplingthe cap to the medical connector can force at least a portion of theantiseptic from the pad and into contact with unsealed portions of thefemale connector. Caps may also be used to seal a fluid pathway of amale connector so as to prevent antiseptic from entering the fluid path.

FIGS. 1-3 illustrate an embodiment of an assembly 100 that can include afemale cap 102 and a male cap 104, each of which can be used to cover aseparate medical connector. The assembly 100 can be provided in apre-use, assembled, or closed state, and the caps 102, 104 can beremoved from each other. In particular, the female and male caps 102,104 can be coupled with each other via a sealing mechanism 189. In theillustrated embodiment, the sealing mechanism 189 comprises a sealingsleeve 191. The terms “coupled” and variants thereof are used in theirordinary sense and include arrangements in which the caps 102, 104directly engage one another when the assembly 100 is in the assembled orpre-use state. The terms also include arrangements such as thatillustrated in FIG. 1, where the caps 102, 104 do not directly contactone another when the assembly 100 is in the assembled or pre-use state,yet are securely held in a fixed relationship relative to one another.Stated otherwise, each of the caps 102, 104 is separately secured to thesealing sleeve 191, and thus, although the caps 102, 104 are spaced fromone another, they nevertheless are coupled or indirectly secured to eachother.

FIG. 2 is an exploded view of the assembly 100. The female cap 102 caninclude a housing 110 into which a support member 134 and a sealingmember 141 are received. As discussed further below, the support member134 can assist the sealing member 141 in the formation of a seal with alumen of a female-type medical connector. For example, in someembodiments, the support member 134 can resist distal movement of thesealing member 141 within the housing 110. In further embodiments, thesupport member 134 may be resiliently deformable, and thus may urge thesealing member 141 in a proximal direction, such as in reaction to adistal movement of the sealing member 141. Accordingly, in someinstances, the support member 134 may also be referred to as a biasingmember. In the illustrated embodiment, the support member 134 comprisesan antiseptic reservoir or pad 132, which is also discussed furtherbelow.

The male cap 104 can include a housing 150 into which a support or post177, an antiseptic reservoir or pad 170, and a sealing member 190 arereceived. As further discussed below, the post 177 and the pad 170 maybe considered as a multi-part support member 176 that is configured toresist movement of the sealing member 190 in a distal direction withinthe housing 150. In further embodiments, one or more of the post 177 andthe pad 170 may be resiliently deformable (e.g., elastomeric) such thatone or more of the post 177 and the pad 170 can urge the sealing member190 toward a proximal end of the male cap 104, such as after the sealingmember 190 has been displaced distally within the housing 150.Accordingly, in some instances, the support member 176 may also bereferred to as a biasing member.

The terms “proximal” and “distal,” when used herein relative to a cap,or components thereof, are used relative to the coupling of the cap witha medical device, such that the medical device is inserted into aproximal end of the cap, or component thereof and advanced toward adistal end of the cap or component. Accordingly, in the illustratedembodiment, the proximal ends of the caps 102, 104 are directed towardeach other and the distal ends of the caps 102, 104 are directed awayfrom each other when the assembly 100 is in the pre-use configuration(see FIG. 1). The female cap 102 can define one or more recesses 116 andthe male cap 104 can define one or more recesses 162 at positions thatare between the proximal and distal ends of the caps 102, 104,respectively.

The sleeve 191 can include end surfaces or edges 196, 198 that areconfigured to interact with the male and female caps 104, 102,respectively. The sleeve 191 can define one or more protrusions 199 thatare configured to be received in the one or more recesses 116 of thefemale cap 102. Each protrusion 199/recess 116 pair can cooperate as adecoupling feature, release mechanism, or separation assist 107.Similarly, the sleeve 191 can define one or more protrusions 197 thatare configured to be received in the one or more recesses 162 of themale cap 104. Each protrusion 197/recess 162 pair can cooperate as aseparation assist 108. The protrusions 197, 199 and recesses 116, 162can have rounded edges (e.g., rounded or radiused valleys and apexes),which can facilitate their rotational movement relative to one another.

As shown in FIG. 3, each protrusion 199 can include a portion of theedge 198 of the sleeve 191. Moreover, each protrusion 199 can define apair of faces 199 a, 199 b that are angled in opposite directions. Here,the term “angled” refers to any suitable non-zero, non-180-degree anglerelative to a transverse cross-sectional plane (not shown) that passesperpendicularly through a central axis of the sleeve 191. For a paththat is traced along the edge 198 in a clockwise direction (when lookingtoward the edge 198), the path moves away from the longitudinal centerof the sleeve 191 along the faces 199 a, and the path moves toward thelongitudinal center of the sleeve 191 along the faces 199 b.

Similarly, each protrusion 197 can include a portion of the edge 196 ofthe sleeve 191, and each protrusion 197 can define a pair of oppositelyangled faces 197 a, 197 b. For a path that is traced along the edge 196in a clockwise direction (when looking toward the edge 196), the pathmoves away from the longitudinal center of the sleeve 191 along thefaces 197 a, and the path moves toward the longitudinal center of thesleeve along the faces 197 b.

The protrusions 197, 199 can be relatively flexible, as they extend agreater distance from the longitudinal center of the sleeve 191, andthus define longer moment arms relative thereto. In some embodiments,the sleeve 191 includes a central band or reinforcing rib 188 that canprovide structural integrity to the sleeve 191 and can prevent orinhibit large deformations of the sleeve 191 during use and/or crushingof the sleeve 191 after removal of one or more of the caps 102, 104therefrom. The illustrated reinforcing rib 188 projects radiallyinwardly at a central region of the sleeve 191. In other embodiments,the reinforcing rib 188 may extend outwardly or may be omitted. Forexample, in some embodiments, the sleeve 191 may define a uniformthickness along its full length.

The sleeve 191 defines an external surface 182 and an internal surface183, each of which extends away from the edges 196, 198. The internalsurface 183 can define a cavity, opening, or lumen 184 into whichproximal ends of the male and female caps 104, 102 can be received. Theterms “external surface” and “internal surface” are used relative to theassembly 100 when it is in the pre-use state (e.g., the configurationshown in FIG. 1). Accordingly, when the assembly 100 is in an assembledstate, the internal surface 183 is at an interior of the assembly 100,so as not to be exposed to an environment that surrounds the assembly100, and the external surface 183 is at an exterior of the assembly,such that it is exposed to the environment and may be grasped orotherwise contacted by a user. It is noted that in the foregoing portionof the present specification, the terms “interior” and “exterior” may attimes be used with respect to inwardly directed surfaces and outwardlydirected surfaces of certain caps, without regard to whether any portionof these surfaces is in fact internal to an assembly that includes thesecaps when the assembly is in the pre-use state. The internal surface 183of the sleeve 191 also can define a connection interface 193 (FIG. 3)and a connection interface 195 by which the caps 104, 102, respectively,can be coupled to the sleeve 191, as discussed further below.

With reference to FIGS. 4A-4C and 6, the housing 110 of the female cap102 can extend between a closed distal end and an open proximal end. Theclosed distal end does not permit any fluid flow therethrough and servesas a barrier between an interior of the housing 110 and an exteriorenvironment. The open proximal end of the housing 110 is configured toreceive at least a portion of a medical connector therein. As discussedfurther below (e.g., with respect to FIG. 9), certain of such medicalconnectors can define an internal female lumen, which may at leastpartially define a fluid line or fluid delivery pathway. The connectorsmay have outwardly disposed threading or some other suitable connectioninterfacing, and the housing 110 may be sized to fit over, or about anoutside of, such an arrangement. The housing 110 can include a sidewall112, which defines the open proximal end, and a base wall 113, whichdefines at least a portion of the closed distal end.

The housing 110 can include a body region 136 near a proximal endthereof, which is substantially cylindrically shaped in the illustratedembodiment. A handle 137 can extend from the body region 136 so as to bepositioned at the distal end of the cap 102. The handle 137 can compriseany suitable gripping features 103, which in illustrated embodimentcomprise opposing gripping regions or grasping platforms 138 that areconfigured to provide a convenient surface against which a user canpress so as to hold and/or twist the cap 102.

As shown in FIG. 4B, the illustrated grasping platforms 138 are mirroredabout a longitudinal plane LP that extends along a central longitudinalaxis A (shown in FIG. 4A) of the housing 110. Each grasping platform 138angles radially inwardly from the body region 136 toward thelongitudinal plane LP, in a proximal-to-distal direction. The graspingplatforms 138 are more steeply angled at their proximal ends than theyare at their distal ends. The angled platforms 138, and particularly thesteeply angled portions thereof, provide convenient surfaces to whichforces may be applied in a distal-to-proximal direction. In theillustrated embodiment, the platforms 138 define two substantiallyplanar regions that are smoothly joined to each other at a roundedtransition. The platforms 138 can define a contour that is substantiallycomplementary to fingertips that are pointed in the proximal direction.

As shown in FIG. 4A, the illustrated grasping platforms 138 also taperinwardly toward the central longitudinal axis A of the housing 110 in aproximal-to-distal direction. In the elevation view that is shown, theplatforms 138 are substantially ovoid. The platforms 138 are sized andshaped to be held between the fingertips of a thumb and another finger(e.g., the index finger) of a user, although other graspingconfigurations may also be efficiently employed with the illustratedarrangement. The platforms 138 provide convenient surfaces to whichtorque may be applied so as to rotate the cap 102 about the longitudinalaxis A.

With reference to FIGS. 4A-4C, the cap 102 can include a lip, rim, orflange 115 that extends radially inwardly at a proximal end of the bodyregion 136. The flange 115 can contact the edge 198 of the sleeve 191 toensure a desired insertion depth of the cap 102 within the sleeve 191.The flange 115 can define the one or more recesses 116 mentioned above.

With reference again to FIG. 4B, each recess 116 can be at leastpartially defined by a pair of faces 116 a, 116 b of the flange 115 thatare angled in opposite directions. The angles can be any suitablenon-zero, non-180-degree angles relative to a transverse cross-sectionalplane TP that passes perpendicularly through the a central axis A of thehousing 110. In particular, the faces 116 a can define an angle αrelative to the transverse plane TP, and the faces 116 b can define anangle β relative to the transverse plane TP. In the illustratedembodiment, the angles α, β are the same, although other arrangementsare possible (as discussed further below). For a path is traced alongthe flange 115 in a clockwise direction (when looking toward the flange115), the path moves proximally along the faces 116 a and the path movesdistally along the faces 116 b. The faces 116 a, 116 b can besubstantially planar over at least a portion thereof, and can beconfigured to complementarily contact the faces 199 a, 199 b,respectively, of the sleeve 191. Additional discussion of the faces 116a, 116 b is provided below with respect to FIGS. 5A-5B.

The housing 110 defines an external surface 118 and an internal surface119, each of which extends away from the flange 115. The internalsurface 119 of the cap 102 can include an outwardly directed surface ofthe sidewall 112, a proximal end 124 of the sidewall 112, and aninwardly directed surface of the sidewall 112 (see FIGS. 4C and 6). Theoutwardly directed portion of the internal surface 119 can define aconnection interface 140 that is configured to interact with or engagethe connection interface 195 of the sleeve 191 so as to connect the cap102 to the sleeve 191. In the illustrated embodiment, the connectioninterfaces 140, 195 couple with each other via a friction-fitengagement. For example, an inner diameter of the connection interface195 of the sleeve 191 can be slightly smaller than an outer diameter ofthe connection interface 140 of the cap 102. The friction fit can besufficiently strong to provide a fluid-tight seal between the cap 102and the sleeve 191, yet can allow the cap 102 to be removed from thesleeve 191 via manipulation by a user (e.g., without the use ofancillary tools). The fluid-tight seal can prevent evaporative loss ofantiseptic from an interior of the assembly 100 when it is in thepre-use configuration and/or can maintain the sterility of the internalportions of the assembly 100. In other or further embodiments, theconnection interfaces 140, 195 can include threads and/or any othersuitable attachment features. In the illustrated embodiment, a proximalportion of the connection interface 195 includes a chamfer 120, whichcan assist in centering the cap 102 relative to the sleeve 191 whenconnecting the cap 102 to the sleeve 191.

The proximal end 124 of the housing 110 (which is also a proximal end ofthe internal surface 119, or more generally, of the sidewall 112), candefine a seal inhibitor 125, which can include one or more contactregions 126 and one or more venting regions 127. In the illustratedembodiment, the seal inhibitor 125 includes two contact regions 126 thatare diametrically opposite from each other, and also includes twoventing regions 127 that are diametrically opposite from each other andare angularly spaced from the contact regions. Other configurations ofthe seal inhibitor 125 are also possible, such as, for example, the sealinhibitors discussed in U.S. patent application Ser. No. 12/610,141,titled STERILIZATION CAPS AND SYSTEMS AND ASSOCIATED METHODS, filed Oct.30, 2009, now published as U.S. Patent Application Publication No.2010/0049170, which was previously incorporated by reference in thisdisclosure. For example, a portion of the seal inhibitor 125 can contactan outwardly projecting surface (e.g., a transverse planar surface) of amedical device with which that cap 102 is coupled. In particular, theproximal end 124 of the cap 102 can contact the surface at two separatecontact regions 126 when the cap 102 is fully coupled with theconnector. In contrast, the venting regions 127 can be spaced from theoutwardly projecting surface of the connector. Such an arrangement canallow venting of antiseptic from a disinfecting chamber 122 defined bythe housing 100, through the venting regions 127, and into thesurrounding environment.

With reference to FIGS. 4C and 6, the inwardly directed portion of theinternal surface 119 of the sidewall 112 can define the disinfectionchamber 122, which can include a connection interface 130. Any suitableconnection system may be used for the connection interface 130. In theillustrated embodiment, the connection interface includes inwardlyprojecting threads 131. The connection interface 130 can be configuredto attach the cap 102 to a medical connector in a secure yet selectivelyremovable manner. For example, the cap 102 can be connected in anysuitable manner with any suitable medical connector. In otherembodiments, the connection interface 130 may include latches or prongsthat are configured to snap over an outwardly extending rib of aconnector, or may include one or more outwardly extending ribs overwhich one or more latches or prongs of the medical connector may snap.

A proximal portion of the disinfection chamber 122 can be larger than adistal extension 123 of the chamber. In the illustrated embodiment, thedisinfection chamber 122 defines three substantially frustoconicalregions. The proximal region has a slightly tapered outer boundary thatdecreases in cross-sectional area in the distal direction; theintermediate region has a more pronounced tapered outer boundary thatmore rapidly decreases in cross-sectional area in the distal direction;and the distal region or distal extension 123 has a slightly taperedouter boundary that decreases in cross-sectional area in the distaldirection at about the same rate as the proximal region. Theintermediate and distal regions correspond with the proximal and distalregions, respectively, of the grasping platforms 138.

The constricted intermediate region of the disinfection chamber 122 canprovide a reactive force to a distal end of the pad 132 when the cap 102is secured to a medical connector. The reactive force can be sufficientto prevent the pad 132 from being forced into the distal extension 123.In the illustrated embodiment, the threads 131 also provide resistiveforces. Axial compression of the pad 132 as the cap 102 is coupled to amedical connector can swab the connector and deliver antiseptic 133 fromthe pad 132 into contact with the medical connector in manners such asdescribed further below. In some embodiments, the pad 132 may beresiliently deformable so as to regain a pre-use shape after a medicalconnector is decoupled from the cap 102. In other embodiments, the pad132 may instead be plastically deformable.

In various embodiments, the pad 132 can be configured to retain anantiseptic 133. For example, the pad 132 can comprise any suitablesponge-like material, such as an elastomeric foam, any open-cell foam,felt, or non-woven fiber matrix, and can be configured to conform to thecontours of a portion of a medical connector that is introduced into thedisinfection chamber 122 (e.g., uneven surfaces of an end of a femaleluer connector of any suitable variety; see also FIGS. 9-10C and theassociated written description). The pad 132 can also comprise anyclosed-cell foam, as well as a solid elastomeric material such assilicone or the like.

The pad 132 can have a series or network of openings or spaces thereinthat can retain the antiseptic 133 when the pad 132 is in an expandedstate. For example, the antiseptic 133 can be received within, occupy,fill (or partially fill), wet, soak, or saturate at least a fraction ofthe pad 132, or stated otherwise, can fill the pad 132 to a givenconcentration level. Compression of the pad 132 can cause antiseptic 133to egress from the pad 132 so as to contact the medical connector.Resilient expansion of the foam upon removal of a compressive force canallow the pad 132 to soak up or absorb at least some of the antiseptic133 that had previously been forced from the pad 132. In someembodiments, the antiseptic 133 can comprise any liquid antiseptic, suchas, for example, alcohol (e.g., isopropyl alcohol) at variousconcentrations (e.g., ranging from 50-90%), ethanol at variousconcentrations (e.g., ranging from 50-95%), and combinations of anyalcohols with any antiseptics, or a dry material, such as chlorhexidine,ethylenediaminetetraacetic acid (EDTA), lodaphors, or any suitablecombination thereof. Accordingly, although the antiseptic 133 isschematically depicted in FIG. 6 as a series of droplets, the antiseptic133 is not necessarily liquid and may fill the pad 132 to a greater orlesser extent than what is shown. In the illustrated embodiment, whenthe assembly 100 is in the pre-use condition, the pad 132 is in arelaxed, expanded, or uncompressed state in a longitudinal direction. Itis noted that the pad 132 may be uncompressed in one or more dimensions,yet compressed in one or more other dimensions, when the assembly 100 isin the pre-use state. For example, the pad 132 can be expanded or in arelaxed state in a longitudinal direction, yet compressed radiallyinwardly via the sidewall 112, when the assembly 100 is in the pre-usestate.

In the illustrated embodiment, the pad 132 is substantially square incross-section along its full longitudinal length when the pad 132 is ina relaxed orientation (see FIG. 2). Such an arrangement can facilitateand/or reduce material costs associated with the manufacture of the pad132. At least a portion of the pad 132 (e.g., the corners thereof) maybe compressed radially when the pad 132 is positioned within the housing112. Other rectangular cross-sections are also possible for the pad 132,and in other or further embodiments, the pad 132 may define arectangular cross-section along only a portion of the longitudinallength thereof. In other embodiments, at least a portion of the pad 132may define a round cross-section, such as a circular, elliptical, orother ovoid shape. For example, the pad 132 can be cylindrical so as tohave a circular cross-section. The pad 132 may define any other suitableshape, and may or may not be radially compressed when the assembly 100is in the pre-use state.

With reference to FIGS. 2 and 6, the sealing member 141 can be formed ofany suitable material, such as, for example, an elastomer (e.g.,silicone) or a thermoplastic, such as polypropylene, polycarbinate,acrylonitrile butadiene styrene (ABS), polyvinyl chloride (PVC), orrigid or semi-rigid thermoset plastic. The sealing member 141 can beformed in any suitable fashion, such as via molding or die cutting. Insome embodiments, the sealing member 141 can be harder, more rigid,and/or less compliant than the pad 132. The sealing member 141 may beintegral to the pad 132. For example, in some embodiments, the sealingmember 141 may comprise a skin that is applied to the pad 132, or maycomprise a modification of a surface of the pad 132 (e.g., melting, heatforming, or the like). In other embodiments, the sealing member 141 maybe adhered to the pad 132 in any suitable fashion.

In the illustrated embodiment, the sealing member 141 is substantiallyconical. Such a shape can be well-suited for coupling with an end of afemale luer connector, as further discussed below. Other shapes of thesealing member 141 are also possible, including, for example, flat orplanar, disk-shaped, spherical, etc. As discussed with respect to otherembodiments, at least a portion of the sealing member 141 may define aluer taper that complies with ISO luer standards (e.g., ISO 594-1:1986and ISO 594-2:1998), such that the sealing member 141 can create aliquid-tight seal with a lumen of a female luer connector.

With reference to FIGS. 5A-5C, the housing 150 of the male cap 104 canextend between a closed distal end and an open proximal end. The closeddistal end does not permit any fluid flow therethrough and serves as abarrier between an interior of the housing 150 and an exteriorenvironment. The open proximal end of the housing 150 is configured toreceive at least a portion of a medical connector therein. Inparticular, the open proximal end of the housing 150 is sized and shapedto receive at least a portion of a male protrusion of a medicalconnector. For example, the open proximal end of the housing 150 can beconfigured to receive at least a portion of a male luer. The housing 150can include a sidewall 152, which defines the open proximal end, and abase wall 154, which defines at least a portion of the closed distalend.

As viewed from the exterior (e.g., in FIGS. 5A and 5B), a shape and/orconfiguration of the distal end of the housing 150 can be similar oridentical to the distal end of the housing 110 of the female cap 102,which is discussed above. For example, in the illustrated embodiment,the housing 150 includes a body region 136 and a handle 137 withgrasping platforms 138, which when viewed exteriorly, are identical tothe identically numbered features of the cap 102. Accordingly, as can beseen in FIGS. 1 and 6, when the assembly 100 is in the pre-use state, anexterior thereof can be symmetrical about three mutually perpendicularplanes. Other arrangements are also possible.

With continued reference to FIGS. 5A-5C, the housing 150 can include alip, rim, or flange 161 that extends radially inwardly at a proximal endof the body region 136. The flange 161 can contact the edge 196 of thesleeve 191 so as to ensure that the cap 104 is inserted into the sleeve191 to the desired depth. The flange 161 can define the one or morerecesses 162 mentioned above.

With reference to FIG. 5B, each recess 162 can be at least partiallydefined by a pair of faces 162 a, 162 b of the flange 161 that areangled in opposite directions. The angles can be any suitable non-zero,non-180-degree angles relative to a transverse cross-sectional plane TPthat passes perpendicularly through the a central axis of the cap 104.In particular, the faces 162 a can define an angle α′ relative to thetransverse plane TP, and the faces 162 b can define an angle β′ relativeto the transverse plane TP. In the illustrated embodiment, the anglesα′, β′ are the same, although other arrangements are possible (asdiscussed further below). Moreover, in the illustrated embodiment, theangles α′, β′ are identical to the angles α, β defined by the faces 116a, 116 b of the cap 102. For a path is traced along the flange 161 in aclockwise direction (when looking toward the flange 161), the path movesproximally along the faces 116 a and the path moves distally along thefaces 116 b. The faces 116 a, 116 b can be substantially planar over atleast a portion thereof, and can be configured to complementarilycontact the faces 197 a, 197 b, respectively, of the sleeve 191.

The male cap 104 defines an external surface 165 and an internal surface166, each of which extends away from the flange 161. The internalsurface 166 of the cap 104 can include an outwardly directed surface ofthe sidewall 152, a proximal end of the sidewall 152, and an inwardlydirected surface of the sidewall 152 (see FIGS. 5C and 6). The outwardlydirected portion of the internal surface 166 can define a connectioninterface 180 that is configured to interact with or engage theconnection interface 193 of the sleeve 191 so as to connect the cap 104to the sleeve 191. The connection interfaces 180, 193 can resemble theconnection interfaces 140, 195 discussed above. In addition, a portionof the sidewall 152 that is at a proximal end of the connectioninterface 180 can include a chamfer 167, which can assist in centeringthe cap 104 relative to the sleeve 191 during connection of thesecomponents.

The sidewall 152 of the cap 104 can define an extension, elongatedportion, or projection 155 that extends proximally from the connectioninterface 180. The projection 155 can be configured to couple with amedical connector that includes a male protrusion. The projection 155includes a connection interface 142 that is configured to effect thecoupling. In the illustrated embodiment, the projection 155 issubstantially cylindrical, and the connection interface 142 comprisesone or more threads 143 that are positioned at an outwardly facingsurface of the cylinder. Any other suitable connection interface 142,such as any of those described above, is possible. In the illustratedembodiment, the reinforcement rib 188 of the sleeve 191 can be at alongitudinal center of the assembly 100, and the projection 155 canextend through the reinforcement rib 188.

With reference to FIGS. 5C and 6, an inwardly directed portion of theinternal surface 166 of the sidewall 152 can define a disinfectionchamber 158, which can extend from the proximal end of the projection155 (i.e., the open proximal end of the cap 104) to the base wall 154. Aproximal portion of the disinfection chamber 158 can include a proximalseal region 171, which can be configured to form a fluid-tight seal withthe male protrusion portion of a medical connector. For example, theseal region 171 may be shaped complementarily to an outer surface of amale protrusion of a medical connector with which the male cap 104 isconfigured to be used. In the illustrated embodiment, the proximal sealregion 171 comprises a substantially frustoconical surface 172 thatcomplies with ISO luer standards (e.g., ISO 594-1:1986 and ISO594-2:1998), such that a portion of a male luer can form a seal with theseal region 171. The frustoconical surface 172 can be tapered so as todecrease in diameter in a distal direction. In other embodiments, theproximal portion of the disinfection chamber 158 may not be configuredto form a fluid-tight seal with a male protrusion of a medicalconnector.

The disinfection chamber 158 can further include an intermediate sealregion 173. In the illustrated embodiment, the intermediate seal regionis formed by a rim, ridge, lip, or shelf 174, which is defined by ashort, substantially frustoconical portion of the sidewall 1052 thatincreases in diameter in the distal direction. An outer edge of aproximal surface of the sealing member 190 can define a greater outerdiameter than a minimum inner diameter of the shelf 174 such that theshelf 174 can maintain the sealing member 190 within the chamber 158.The shelf 174 also can cooperate with the sealing member 190 to seal thechamber 158 when the assembly 100 is in the pre-use state, as furtherdiscussed below.

In the illustrated embodiment, a long distal extension 175 of thedisinfection chamber 122 can extend distally from the shelf 174. Thedistal extension 123 has a slightly tapered outer boundary thatgradually decreases in cross-sectional area in the distal direction. Thedisinfection chamber 122 can include a support column 168 within adistal region thereof. The support column 168 can be integrally formedwith both the base wall 154 and the sidewall 152, and can provide arigid surface against which the post 177 can rest. The support column168 can act as a stop that prevents the post 177 from moving distallywithin the chamber 122 past a proximal end of the column 168. In someinstances, however, a distal portion of the post 177 may deform so as toextend distally slightly past the proximal end of the support column 168when a medical connector is coupled with the cap 104. The support column168 can reduce the amount of material that might otherwise be used toform the handle 137 portion of the cap 104.

The post 177, which may also be referred to as a support or a baseelement, can be configured to provide a base against which theantiseptic reservoir or pad 170 can be compressed so as to forceantiseptic 133 thereform. Accordingly, the post 177 can be harder,stiffer, or less compliant than the pad 170, and can be configured tocompress, under a given force, to a smaller extent than the pad 170 doesunder the same force. For example, in various embodiments, the post 177can be no less than about 2, 3, or 4 times harder than the pad 170.

The post 177 can be elastically deformable such that compression of thepost 177 from a relaxed orientation gives rise to a restorative force.The post 177 can naturally return to the relaxed orientation uponremoval of the compressive force. The post 177 can comprise any suitableelastically deformable material. In some embodiments, the post 177comprises an elastomeric material, such as silicone. In certainembodiments, the post 177 comprises a closed configuration (e.g., closedcell foam) or is otherwise nonabsorbent such that little or noantiseptic 133 that is expelled from the pad 170 is received into thepost 177. In other or further embodiments, the post 177 may comprise aspring (e.g., a compression coil spring).

In the illustrated embodiment, a distal end of the post 177 seats snuglyagainst the inner surface 166 of the sidewall 152. The post 177 may forma fluid-tight seal with the sidewall 152, which may prevent antiseptic133 that is expelled from the pad 170 from migrating into the distalregions of the disinfecting chamber 158. Rather, the antiseptic 133 canbe restrained to the proximal regions of the disinfecting chamber 158where it can be urged into contact with a male protrusion of a medicalconnector.

The pad 170 can comprise any suitable material, such as those describedabove with respect to other pads (including plastically deformablematerials, in some instances), and may be elastically or resilientlydeformable. In some embodiments, the pad 170 is attached to the post 177via any suitable adhesive or other attachment mechanism, although inother embodiments, no such attachment mechanisms are used. For example,the pad 170 and the post 177 may be maintained in contact with eachother due to a slight longitudinal compression of one or more of thesecomponents once the cap 104 is assembled (e.g., once the post 177, thepad 170, and the sealing member 190 are positioned between the supportcolumn 168 and the shelf 174). Similarly, the pad 170 may be attached tothe sealing member 190, or it may maintain a substantially fixedorientation relative to the sealing member 190 without such attachmentdue to the resilience of the pad 170 and/or the post 177, which are in aslightly compressed state.

In the illustrated embodiment, the pad 170 is substantially square incross-section along its full longitudinal length when the pad 170 is ina relaxed orientation (see FIG. 2). Such an arrangement can facilitateand/or reduce material costs associated with the manufacture of the pad170. At least a portion of the pad 170 (e.g., the corners thereof) maybe compressed radially when the pad 170 is positioned within the housing152. Other rectangular cross-sections are also possible for the pad 170,and in other or further embodiments, the pad 170 may define arectangular cross-section along only a portion of the longitudinallength thereof. In other embodiments, at least a portion of the pad 170may define a round cross-section, such as a circular, elliptical, orother ovoid shape. For example, the pad 170 can be cylindrical so as tohave a circular cross-section. The pad 170 may define any other suitableshape, and may or may not be radially compressed when the assembly 100is in the pre-use state.

As previously mentioned, the pad 170 and the post 177 can, in someembodiments, cooperate as a two-part support member 176. It is to beunderstood that any other suitable support members 176 may be used. Insome embodiments, one or more of the pad 170 and post 177 may beplastically deformable, such that the support member 176 is merelycompressible. In other embodiments, such as that illustrated in thepresent drawings, the pad 170 and the post 177 can be resilientlydeformable such that a restorative force arises when the support member176 is compressed. The support member 176 thus may also be referred toas a biasing member 176, in certain instances.

In the illustrated embodiment, the biasing member 176 can urge thesealing member 190 in the proximal direction into sealing contact withthe shelf 174. The seal thus formed may be fluid-tight, and may preventantiseptic 133, whether in liquid or vapor form, from exiting thedisinfecting chamber 158 through the proximal end of the cap 104 priorto coupling of the cap 104 to a medical connector. This proximal sealmay be in place when the assembly 100 is in the pre-use configuration,as well as after the separation of the male and female caps 104, 102when the assembly 100 is opened.

The illustrated sealing member 190 comprises unitary piece of materialthat includes a cylindrical region and a conical region. The conicalregion can be well-suited to form a seal with a tip of the projection ofa male medical connector in manners such as described above. In someinstances, an apex of the conical region can be received within a lumenof a luer when a medical connector is coupled with the cap 104 (see,e.g., FIG. 8A). The sealing member 190 can be formed of any suitablematerial, such as, for example, an elastomer (e.g., silicone) or athermoplastic, such as polypropylene, polycarbinate, acrylonitrilebutadiene styrene (ABS), polyvinyl chloride (PVC), or rigid orsemi-rigid thermoset plastic. The sealing member 190 can be formed inany suitable fashion, such as via molding or die cutting. In someembodiments, the sealing member 190 can be harder, more rigid, and/orless compliant than the pad 170. The sealing member 190 may be integralto the pad 170. For example, in some embodiments, the sealing member 190may comprise a skin that is applied to the pad 170, or may comprise amodification of a surface of the pad 170 (e.g., melting, heat forming,or the like). Other shapes of the sealing member 190 are possible,including, for example, flat or planar, disk-shaped, spherical, etc.

FIGS. 7A and 7B illustrate stages in a method of removing the male cap104 from the assembly 100. In some embodiments, it can be particularlyadvantageous to use the separation assists 108 in the removal process.For example, in some instances, the fluid-tight seal between the cap 104and the sleeve 191 can be relatively tight and/or a slight vacuum may bepresent within the assembly 100 (and/or may arise as the cap 104 isremoved from the assembly 100), such that the separation assists 108 canfacilitate removal of the cap 104.

FIG. 7A illustrates the assembly 100 in the pre-use state, with thefaces 162 a, 197 a and 162 b, 197 b of the surfaces 161, 196 in contactwith each other. Each paired set of surfaces constitutes a separationassist 108. In the illustrated embodiment the assembly 100 includes fourseparation assists 108 rotationally spaced from each other at intervalsof approximately 90 degrees. Focusing now on the upper separation assist108 that includes the faces 162 b, 197 b, the face 162 b can define anangle β′ (see FIG. 5B) of about 20 degrees. The face 197 b of the sleeve191 is at the same angle, although oppositely directed.

In order to separate the cap 104 from the sleeve 191, the cap 104 can berotated relative the sleeve 191. In the illustrated embodiment, the cap104 is rotated counterclockwise, which can cause the faces 162 b, 197 bto interact with each other and slide past each other. The cap 104 thuscams relative to the sleeve 191 as the rotational motion is convertedinto translational movement of the cap 104 away from the sleeve 191, asshown by the arrow in FIG. 7B.

Where the angles α′, β′ (see FIG. 5B) of the surfaces 162 a, 162 b areidentical, the same mechanical advantage may be present whether the cap104 is rotated in the clockwise or counterclockwise directions. In otherembodiments, the separation assists 108 can be configured to aid inseparating the cap 104 from the sleeve 191 only when the cap 104 isrotated in one predetermined direction (e.g., either clockwise orcounterclockwise). For example, the pair of faces 162 a or the pair offaces 162 b may define an angle α′ or β′, respectively, of 20 degrees soas to allow separation as shown in FIG. 5B, whereas the other pair offaces 162 a, 162 b may be at an angle of about 90 degrees (i.e.,approximately parallel to or extending through a central axis of the cap104) so as to prevent rotation and separation of the cap 104. In otherembodiments, one or more of the faces 162 a, 162 b may be at larger orsmaller angles α′, β′. For example, one or more of the angles α′, β′ maybe no more than about 15, 20, 1, 45, 60, or 75 degrees or no less thanabout 15, 20, 1, 45, 60, or 75 degrees. Other configurations of theseparation assists 108 are also possible. For example, in someembodiments, the complementary surfaces of the recess 162 and theprotrusion 199 can define angles as just described, but the surfaces maybe rounded or otherwise non-planar.

The foregoing discussion regarding the separation assists 108 appliesequally to the separation assists 107. In the illustrated embodiment,the separation assists 107, 108 are substantially identical. The sleeve191 may be reversible, as either end thereof may connect with either cap102, 104. In other embodiments, the arrangements of the separationassists 107, 108 may be different from each other. For example, theplanar surfaces of the separation assist 107 may be at a larger orsmaller angle than those of the separation assist 108 so as to provide adifferent amount of separation force. Moreover, in some embodiments, theassembly 100 includes a number of separation assists 107 equal to thenumber of separation assists 108, whereas in other embodiments, theassembly 100 may include more or fewer separation assists 107 ascompared with the number of separation assists 108. Other arrangementsof the separation assists 107, 108 are contemplated, including thosediscussed above with respect to the assembly 2700. Other embodiments maybe devoid of the separation assists 107, 108. Moreover, in someinstances, a user may remove one or more of the caps 102, 104 from theassembly 100 in a substantially longitudinal direction only (e.g.,without rotating the caps 102, 104 relative to each other).

FIGS. 8A-8D illustrate consecutive stages of the cap 104 being coupledwith a medical device 200 that includes a male protrusion 219, which inthe illustrated embodiment is a male luer 220. As mentioned above, otherarrangements of the male protrusion 219 are also contemplated. A tip 221of the protrusion 219, can be received within the disinfection chamber158 prior to contacting the sealing member 190. Stated otherwise, thesealing member 190 can be recessed relative to a proximal end of thesidewall 152 by a distance that is sufficiently great to permit at leasta portion of the male luer 220 to be received within the sidewall 152before the male luer contacts the sealing member 190.

In the illustrated stage of the procedure, the luer 220 has beenadvanced sufficiently far into the disinfection chamber 158 to contactthe sealing member 190 and to form a seal therewith. The connectioninterface 142 of the cap 104 has not yet engaged a connection interface212 of the medical connector 200 at this stage, and the sealing member190 is just beginning to move from its initial orientation, or position,in a distal direction within the disinfection chamber 158 so as to breakthe proximal seal between the sealing member 190 and the shelf 174. Thesupport member 176, which is also in an initial orientation, can resistsuch distal movement of the sealing member 190, which resistive forcecan be sufficient to create the seal between the sealing member 190 andthe luer 220 and thereby seal the fluid path 222.

In FIG. 8B, the luer 220 has been advanced slightly further into thedisinfection chamber 158, thereby compressing the pad 170 somewhat andforcing antiseptic 133 out of the pad 170. The sealing member 190 candefine an outer diameter that is smaller than an inner diameter of thisportion of the disinfection chamber 158 such that a fluid path ispresent about an exterior of the sealing member 190. Stated otherwise,the sealing member 190 has been urged distally to a position where aperiphery or outermost perimeter of the sealing member 190 is spacedfrom the sidewall 152 such that an opening, spacing, or gap that existsbetween the sealing member 190 and the sidewall 152. This opening mayfunction as a fluid port.

Antiseptic 133 thus can flow about the sealing member 190 and/or anyother portion of an open region that exists between the inner surface166 of the sidewall 152 and the outer surfaces of the post 177, the pad170, the sealing member 190, and the luer 220. Further advancement ofthe luer 220 into the disinfection chamber 158 can cause the antiseptic133 to fill this open region. However, the antiseptic 133 does not enterinto a fluid path, fluid passageway, or lumen 222 of the luer 220 due tothe seal between the luer 220 and the sealing member 190. Furtheradvancement of the luer 220 into the disinfection chamber 158 also canstrengthen the seal between the luer 220 and the sealing member 190 dueto the increasing restorative forces that arise as the pad 170 iscompressed.

As the pad 170 is softer or more compliant than the post 177, the pad170 has been compressed to a much greater extent than the post 177 atthis stage. Indeed, in some embodiments, the post 177 may compress onlyslightly or not at all at this stage.

In the illustrated embodiment, the interfaces 142, 212 have not yetcoupled with each other at this stage. However, in other embodiments,the interfaces 142, 210 may already cooperate with each other at this orat a previous stage so as to draw the luer 220 into the disinfectionchamber 158.

In FIG. 8C, the luer 220 has been advanced even further into thedisinfection chamber 158, thereby compressing the pad 170 to a greaterextent and forcing additional antiseptic 133 into the interior regionsof the disinfection chamber 158. In the illustrated embodiment, the post177 is shown as having been slightly compressed relative to itsconfiguration in the stage shown in FIG. 8C, whereas the pad 170 hasbeen nearly completely compressed, such that all or nearly all of theantiseptic 133 has been forced therefrom. Cooperation between theconnection interfaces 142, 212 can facilitate compression of the pad 170and/or the post 177.

Although the outer surface of the luer 220 appears to be nearly parallelto and in contact with the luer-tapered surface 172 of the sidewall 152,a fluid-tight seal may not have formed yet in this area. Accordingly,the antiseptic 133 may be permitted to cover the portion of the luer 220that is within the chamber 158, while in some embodiments, a smallportion of antiseptic 133 may also be permitted to exit from thedisinfection chamber 158. The portion of the luer 220 that is within thedisinfection chamber 158 thus may contact the antiseptic 133 so as to bedisinfected thereby.

FIG. 8D illustrates a final or fully coupled stage or an end-of-strokeorientation, in which the sealing member 190 has been moved distallywithin the chamber 158 to a retracted orientation. The retractedorientation thus can correspond with a final position of the sealingmember 190 when the medical connector 200 has been fully coupled withthe cap 104. When it is in the retracted orientation, the sealing member190 is spaced from the proximal end of the sidewall 152 by a greaterdistance than it was when in the initial orientation shown in FIG. 8A.Stated otherwise, the sealing member 190 can been moved from the initialorientation (FIG. 8A) to the retracted orientation (FIG. 8D) so as tospace the sealing member 190 from the connection interface 142 by aprogressively greater amount. Similarly, or correspondingly, the supportmember 176 can been moved from the initial orientation (FIG. 8A) to theretracted orientation (FIG. 8D) so as to space a proximal end of thesupport member 176 from the connection interface 142 by a progressivelygreater amount. In some instances, the initial and retractedorientations may be described relative to the connection interface 142,since the connection interface 212 of the medical connector 200 and theconnection interface 142 of the cap 104 can cooperate with each other toadvance the luer 220 deeper into the chamber 158, and as a result,advance the sealing member 190 and the support member 176 to deeperpositions within the disinfecting chamber 158.

In the illustrated embodiment, when the sealing member 190 has reachedthis retracted orientation, the luer 220 has been advanced even furtherinto the disinfection chamber 158 such that the luer 220 forms a sealwith the luer-tapered surface 172 of the sidewall 152. Antiseptic 133can be retained in all open portions of the disinfection chamber 158that are between the seal formed by the luer 220 and the sealing member190 and the seal formed by the luer 220 and the sidewall 152. In theillustrated embodiment, a relatively large portion of the luer 220,which includes all or most of the tip 221, is in continual contact withthe portion of the antiseptic 133 thus retained. This portion of theluer 220 can be bathed by the antiseptic 133 and disinfected thereby. Inother embodiments, larger portions of the luer 220 can be bathed.

The deformable nature of the post 177 can allow for distal movement ofthe pad 170, even after the pad 170 has been fully compressed. Such anarrangement can allow for a range of acceptable lengths and diametersfor the luer 220. For example, shorter luers 220 than that illustratedin the drawings may still be able to fully compress the pad 170 so as toexpel all antiseptic therefrom.

In other embodiments, the medical connector 200 may include a maleprotrusion other than a luer 220, such as a male protrusion that isshaped substantially as a cylinder or in some other configuration, suchas a taper having dimensions other than those of a standard luer. Insome embodiments, the surface 172 may be shaped complementarily to theouter surface of such protrusions so as to for a seal therewith. Instill other embodiments, the sidewall 152 may not form a seal with theprotrusion.

When the luer 220 is removed from the chamber 158, the restorationforces of the pad 170 and/or the post 177 (i.e., the resilient biasingmember 176) can maintain the seal between the luer 220 and the sealingmember 190, which can prevent antiseptic from entering into the lumen222 of the luer 220. The sealing member 190 can be returned to theinitial orientation shown in FIG. 8A.

FIG. 9 illustrates an embodiment of a medical connector assembly 300with which the female cap 102 can be coupled. Any suitable medicalconnector or medical connector assembly is contemplated, particularlythose that define one or more open female lumens. The illustratedmedical connector assembly 300 comprises a medical stopcock valveassembly that includes a plurality of fluid-directing tubes, each havinga connection interface. The connector assembly 300 can be formed of anysuitable material, such as, for example, plastic. In the illustratedembodiment, the assembly 300 comprises a first port or female connectorportion 301 and a second port or female connector portion 302 that canbe placed in selective communication with a third port or male connectorportion 303 via a valve or direction control member 304. The directioncontrol member 304 is rotatably arranged within the valve body forselectively closing one or more ports while opening communicationbetween at least two other ports. The medical connector assembly 300 maybe used in any of a variety of medical procedures and operations, suchas, for example, metering the infusion of fluids into patients. A femalecap 102 can be used with one or more of the female connector portions301, 302, such as when the respective female connector portion or portis not in use.

In the illustrated embodiment, the female connector portions 301, 302each comprise a female luer lock fitting, although other arrangementsare also possible. With reference in particular to the port or connector302, the connector 302 can include a sidewall 310 that includes aconnection interface 312 at a proximal end thereof. The Connectioninterface 312 can include any suitable arrangement, and can beconfigured to cooperate with the connection interface 130 of a femalecap 102 so as to couple the cap to the connector 302 in a secure yetselectively removable manner. In the illustrated embodiment, theconnection interface 312 comprises threading 313. The sidewall 310 candefine a proximal end or proximal face 321 and an interior surface 323.The interior surface 323 can define an open female lumen 322, which candefine a fluid path or passageway through which fluids can flow throughthe assembly 300.

FIGS. 10A-10C illustrate consecutive stages of the cap 102 being coupledwith the port 302 of the connector assembly 300. The coupling mayproceed in a manner similar to coupling the cap 104 with a male medicalconnector 200, as discussed above with respect to FIGS. 8A-8D.

With reference to FIG. 10A, the connection interface 130 of the housing110 can be coupled with the connection interface 312 of the port 302. Insome embodiments, this coupling can take place before contact between aproximal end of the port 302 and the sealing member 141 occurs. The cap102 can be rotated relative to the port 302 so as to further engage thethreads 131, 313 and advance the cap 102 over the port 302. Uponsufficient advancement of the cap 102 over the port 302, the sealingmember 141 can contact the proximal face 321 and/or the interior surface323 of the port 302. In the illustrated embodiment, the sealing member141 initially contacts a ring of the port 302 at which the proximal face321 and the interior surface 323 meet.

In the illustrated stage of the procedure, the port 302 has beenadvanced sufficiently far into the disinfection chamber 122 to contactthe sealing member 141 and to form a seal therewith. The sealing member141 is just beginning to move from its initial orientation, or position,in a distal direction within the disinfection chamber 122. The pad 132,acting as the support member 134, opposes the distal movement of thesealing member 141, thereby providing sufficient resistive force for thecreation of the seal. As shown in FIG. 10A, the support member 134 isalso in an initial orientation. Substantially no antiseptic 133 has beenexpelled from the pad 132 at this stage.

In FIG. 10B, the port 302 has been advanced slightly further into thedisinfection chamber 122, thereby compressing the pad 132 somewhat andforcing antiseptic 133 out of the pad 132. The sealing member 141 candefine an outer diameter that is smaller than an inner diameter of thisportion of the disinfection chamber 122 such that a fluid path ispresent about an exterior of the sealing member 132. Stated otherwise,the sealing member 141 has been urged distally to a position where aperiphery or outermost perimeter of the sealing member 141 is spacedfrom the sidewall 112 such that an opening, spacing, or gap that existsbetween the sealing member 141 and the sidewall 112. This opening mayfunction as a fluid port.

Antiseptic 133 thus can flow about the sealing member 141 and intocontact with the port 302. However, the antiseptic 133 does not enterinto the fluid path 322 of the port 302 due to the seal between the port302 and the sealing member 141. Further advancement of the port 302 intothe disinfection chamber 122 also can strengthen the seal between theport 302 and the sealing member 141 due to the increasing restorativeforces that arise as the pad 132 is compressed.

In the illustrated embodiment, only a relatively small contact area ismaintained between the sealing member 141 and the port 302, but thisarea can be sufficient to form and maintain a fluid-tight seal thatprevents antiseptic 133 from entering the fluid path 322. In otherembodiments, the sealing member 141 can be configured to plug the fluidpath 322 and/or contact a larger portion of the inner surface 323, asdiscussed further below with respect to FIGS. 12-15.

FIG. 10C illustrates a final or fully coupled stage or an end-of-strokeorientation, in which the sealing member 141 has been moved distallywithin the chamber 122 to a retracted orientation. The retractedorientation thus can correspond with a final position of the sealingmember 141 when the cap 102 has been fully coupled with the port 302.When it is in the retracted orientation, the sealing member 141 isspaced from the proximal end of the housing 110 by a greater distancethan it was when in the initial orientation shown in FIG. 10A. Statedotherwise, the sealing member 141 can been moved from the initialorientation (FIG. 10A) to the retracted orientation (FIG. 10C) so as tospace the sealing member 141 from the connection interface 130 by aprogressively greater amount. Similarly, or correspondingly, the supportmember 134 can be moved to a retracted orientation in which it has beencompressed such that a proximal end thereof is further from theconnection interface 130 than it was when the support member 134 was inits initial orientation. In some instances, the initial and retractedorientations may be described relative to the connection interface 130,since the connection interface 130 of the cap 102 and the connectioninterface 312 of the port 302 can cooperate with each other to advancethe port 302 deeper into the chamber 122, and as a result, advance thesealing member 141 and the proximal end for the support member 134 todeeper positions within the chamber 122.

In the illustrated embodiment, when the sealing member 141 has reachedthis retracted orientation, the port 302 has been advanced even furtherinto the disinfection chamber 122. Antiseptic 133 can be permitted toflow to all open portions of the disinfection chamber 122, and thus maybathe, disinfect, or clean an exterior surface of the port 302.

When the port 302 is removed from the chamber 122, the restorationforces of the pad 132 can maintain the seal between the port 302 and thesealing member 141, which can prevent antiseptic from entering into thelumen 322. The sealing member 141 can be returned to the initialorientation shown in FIG. 10A.

FIGS. 11-15 illustrate another embodiment of an assembly 400 thatincludes an embodiment of a female cap 402 and an embodiment of a malecap 404, which can resemble the assembly 100 and caps 102, 104 describedabove in certain respects. Accordingly, like features are designatedwith like reference numerals, with the leading digits “1” incremented to“4.” Relevant disclosure set forth above regarding similarly identifiedfeatures thus may not be repeated hereafter. Moreover, specific featuresof the assembly 400 may not be shown or identified by a referencenumeral in the drawings or specifically discussed in the writtendescription that follows. However, such features may clearly be thesame, or substantially the same, as features depicted in otherembodiments and/or described with respect to such embodiments.Accordingly, the relevant descriptions of such features apply equally tothe features of the assembly 400. Any suitable combination of thefeatures and variations of the same described with respect to theassembly 100 can be employed with the assembly 400, and vice versa. Suchdisclosure methods apply to additional embodiments disclosed hereafter,such as those shown in each of FIGS. 16-19B, 20, 21, 22, 23A-23C, and24.

The caps 402, 404 can be coupled to each other via a sleeve 491. In theillustrated embodiment, the assembly 400 is devoid of separationassists, such as those described above with respect to the assembly 100.

As shown in FIG. 12, the female cap 402 can include a seal inhibitor 425that resembles the seal inhibitor 125 described above. However, the sealinhibitor 425 can define a slightly different shape. In particular, thecontact regions 126 and the venting regions 127 can define acastellation pattern. In other or further embodiments, the cap 402 maybe devoid of a seal inhibitor 425, since, for example, certain medicalconnectors with which the cap 402 may be coupled may not have outwardlyprojecting surfaces against which a seal may be formed at the distal endof the female cap 402 (see, e.g., FIGS. 14 and 15).

With reference to FIG. 15, the cap 402 can include a support member 434that comprises a pad 432, such as the support member 134 and pad 132described above. With reference to FIGS. 12-15, and in particular, FIG.15, the cap 402 can include a sealing member 441 that resembles andfunctions similarly to the sealing member 141 described above, but thatdefines a different shape. The sealing member 441 may be more plug-likethan the sealing member 441, in that it can be configured to contact agreater portion of an interior surface 323 of the female connector orport 302. The sealing member 441 can include a base region 444, atapered region 445, and a proximal flange region 446. In the illustratedembodiment, the base region 444 defines a greater maximum diameter thando the tapered region 445 and the flange region 446. The maximumdiameter of the tapered region 445 can be larger than an inner diameterof the port 302 at the proximal end 321 thereof. The base region 444 mayprevent direct contact with the pad 434, in some embodiments.

The tapered region 445 can be configured to form a seal along asignificant length of the interior surface 323 of the port 302, whichcan ensure that antiseptic is not introduced into the fluid path 322. Insome embodiments, the interior surface 323 of the port 302 and thetapered region 445 of the sealing member 441 each conform to standardISO luer specifications, such that a fluid-tight seal is formed once thecap 402 has been advanced over the port 302 by a sufficient amount. Insome embodiments, the proximal flange 446 may be flexible, particularlyin a distal direction. The proximal flange 446 may, in furtherembodiments, define an outer diameter that is slightly larger than anouter diameter defined by a proximal end of the tapered region 445. Theproximal flange 446 may enhance a strength of the seal formed by thesealing member 441 and/or facilitate entry of the sealing member 441into the female lumen defined by the port 302.

FIGS. 16-19B illustrate another embodiment of a female cap 502, whichcan be compatible with various cap assemblies disclosed herein. The cap502 can include a housing 510 that includes a sidewall 512 and an basewall 513. As shown in FIG. 16, a distal end of the housing 510 caninclude gripping features 503 that are shaped differently from thegripping features 103. In the illustrated embodiment, the grippingfeatures 503 comprise tear-shaped depressions. A proximal end of thehousing can include seal inhibitors 525, which can resemble any of theseal inhibitors discussed above.

With reference to FIG. 18, the housing 510 can further define a centralpost 509 that extends proximally from the base wall 513. The post 509provide for a disinfecting chamber 522 that has a smaller volume, ascompared with other female caps described above. Further, a pad 532 thatis disposed at a distal end of the chamber 522 can define asubstantially annular shape, and may comprise less material than certainother embodiments of pads described herein.

The post 509 can include multiple regions, which may have different orspecific functions. In the illustrated embodiment, a proximal region 521of the post 509 can be somewhat thicker than other portions thereof. Theproximal region 521 can define a sealing member 541 portion of the cap502. An outward portion of the proximal region 521 thus may beconfigured to plug and/or seal a female lumen of a medical connector,and thus may, in further embodiments, have a luer-shaped taper (althoughother configurations are also possible).

A medial region 517 of the post 509 may extend distally from theproximal region 521, and may narrow in thickness in the distal directiontoward a folding, bending, crumpling, or weakened region 514. Theweakened region 514 may define a minimum thickness of the post 509. Inthe illustrated embodiment, the weakened region 514 is a circular regionthat extends about a periphery of the post 509. A distal region 511 canextend distally from the weakened region 514, and can increase inthickness in the distal direction. Together, the medial region 517, theweakened region 514, and the distal region 511 can cooperate as a stressconcentrator and may be configured to collapse. These regions may definea support member 534 that is configured to support the sealing member541 sufficiently to permit the sealing member to form a seal with amedical connector, and then collapse upon application of a sufficientamount of force to permit the sealing member 541 to move distally andallow contact between the medical connector and the pad 532, asdiscussed hereafter. The support member 534 can be configured tocollapse upon application of a predetermined amount of force thereto. Insome embodiments, deformation of the support member 534 may resemble thedeformation that occurs when a thin-walled aluminum can (e.g., for softdrinks) is compressed and torqued.

The support member 534 can be plastically deformable, or substantiallyplastically deformable, such that little restorative forces arise afterthe support member 534 has collapsed. In other embodiments, thecollapsible support member 534 may be resiliently deformable. The post509 may be integrally formed with the remainder of the housing 510, orit may be attached thereto. The post 509 and/or the remaining portionsof the housing 510 can be formed of any suitable material. In variousembodiments, the post 509 and/or the housing 510 can comprise anysuitable form of injection moldable, medical grade plastic, including,for example, polypropylene, polyethylene, polycarbonate, polyurethane,ABS, thermoplastic materials, thermoplastic elastomers, etc.

FIG. 19A depicts an early stage of a procedure for coupling the femalecap 502 with a medical connector, such as the port 302. In theillustrated embodiment, connection interfaces of the cap 502 and theport 302 are used to tighten the cap 502 onto the port 302. The sealingmember 541 can form a fluid-tight seal with an interior surface 323 ofthe port 302. A relational geometry of the sealing member 541 and thepad 532 can be such that the seal is formed before any portion of theport 302 contacts the pad 532. Accordingly, in the illustratedembodiment, a distal end of the port 302 is spaced from the pad 532after the seal has been formed. The resistance forces to insertion ofthe port 302 into the cap 502 provided by the support member 534 thuscan be sufficient to allow creation of the seal.

FIG. 19B depicts a later stage of the coupling procedure. The port 302has been inserted further into the cap 502 so as to compress the pad 532and expel antiseptic therefrom. The relative orientation of the sealingmember 541 and the connector 302 is relatively unchanged. However, theadditional compressive forces imparted to the support member 534 as theport 302 is advanced to this position overwhelm the support member 534and cause it to collapse. In particular, the medial region 517 and thedistal region 511 fold inward about the weakened region 514.

The configuration shown in FIG. 19A can be referred to as an initialorientation of each of the sealing member 541 and the support member534. The configuration shown in FIG. 19B can be referred to as aretracted orientation of each of the sealing member 541 and the supportmember 534. When in the retracted orientation, each of the sealingmember 541 and the support member 534 has moved distally relative to aconnection interface 530 defined by the female cap 502.

FIG. 20 illustrates another embodiment of a female cap 602, which can becompatible with various cap assemblies disclosed herein. The cap 602 caninclude a housing 610 that includes a sidewall 612 and an base wall 613.The sidewall 612 can define a connection interface 630 that includesinwardly directed threads 632. The sidewall 612 can also define adisinfecting chamber 622.

The cap 602 includes a sealing member 641, which can resemble othersealing members discussed herein. In the illustrated embodiment, thesealing member 641 can be configured to plug a portion of a female lumenof a medical connector. The sealing member 641 can define asubstantially frustoconical shape.

The cap 602 can include a pad 632 that retains an antiseptic therein. Inthe illustrated embodiment, the pad 632 substantially defines anannulus, and can extend about a support member 634. In particular, thepad 632 can define a cavity 635 through which the support member 634extends.

The support member 634 can be resiliently deformable. In the illustratedembodiment, the support member 634 comprises a coil spring 647. In otherembodiments, the support member 634 can comprise one or more springsthat are in forms other than helical, such as, for example, beam, leaf,conical, torsion, etc. Such springs may comprise any suitable material,such as, for example, metals and/or polymers. The spring 647 can extendbetween the base wall 613 of the housing 610 and the sealing member 641.In the illustrated embodiment, a distal end of the sealing member 641 islongitudinally spaced from (e.g., is positioned above) a proximal end ofthe pad 632.

In use, the sealing member 641 of the cap 602 forms a seal with a femalelumen of a medical connector. After formation of the seal, a distal endof the medical connector can come into contact with the pad 632 so as tocompress the pad 632 and expel antiseptic therefrom. This contact canalso serve to swab the portion of the medical connector that contactsthe pad 632. Each of the sealing member 641 and the support member 647thus can transition from the initial orientation shown in FIG. 20 to aretracted orientation, in which the sealing member 641 and the supportmember 647 are closer to the base wall 613. In transitioning to theretracted orientation, at least a portion of the sealing member cantravel through a portion of the cavity 635 defined by the pad 632. Upondecoupling of the cap 602 from the medical connector, the support member647 can return to its initial orientation, and can also urge the sealingmember 641 back to the initial orientation.

FIG. 21 illustrates another embodiment of a female cap 702, which can becompatible with various cap assemblies disclosed herein, and canparticularly resemble the cap 602. The cap 702 can include a housing 710with a base wall 713 such as the housing 610 and base wall 613, a pad732 such as the pad 632, and a sealing member 741 such as the sealingmember 641. However, the cap 702 can include a support member 734 thatcomprises a compressible pad 748. In some embodiments, the pad 748 isplastically deformable, and in other embodiments, the pad is resilientlydeformable. The resiliently deformable embodiments can operatesubstantially the same as support member 647 described above.

FIG. 22 illustrates another embodiment of a female cap 802, which can becompatible with various cap assemblies disclosed herein, and canparticularly resemble the cap 602. The cap 802 can include a housing 810with a base wall 813 such as the housing 610 and base wall 613, a pad832 such as the pad 832, and a sealing member 841 such as the sealingmember 641. However, the cap 802 can include a support member 834 thatcomprises one or more collapsible extensions 849. In some embodiments,the extensions comprise molded parts, which may be integral with thehousing 810 or attached thereto. In some embodiments, the extensions 849are plastically deformable, and in other embodiments, they areresiliently deformable. The resiliently deformable embodiments canoperate substantially the same as support member 647 described above.

FIGS. 23A-23C illustrate another embodiment of a female cap 902 that isconfigured for connection to a medical connector 302, which includes aconnection interface 312 and defines a female lumen 322. The cap 902 caninclude a housing 910 that defines a connection interface 930, adisinfecting chamber 922, and a distal cavity or chamber extension 925.The chamber extension 925 can extend the disinfecting chamber 922distally. A sidewall of the chamber extension 925 can include lockingfeatures, such as detents or, in the illustrated embodiment, grooves928, 929. In particular, a proximal groove 928 and a distal groove 929are defined, although more grooves are possible. The grooves may extendabout at least a portion of a periphery of the chamber extension 925.

The cap 902 can include a shuttle or plug 921 that is configured totranslate within the chamber extension 925. An annular pad 932 canextend about that plug 921. The plug 921 can include a sealing member941 and a support member 934. In the illustrated embodiment, the sealingmember 941 and support member 934 are integrally formed from the samepiece of material. Other arrangements are also possible.

In some embodiments, the support member 934 can include a relief groove931, which can allow for radial compression of the support member 934and may permit the support member 934 to be under tension when it iswithin the chamber extension 925. The support member 934 can definelocking features that are complementary to those of the chamberextension 925. For example, in the illustrated embodiment,t he supportmember 934 defines outwardly projecting detents 951 that are sized to bereceived within either of the grooves 928, 929. Together, the detents951 and grooves 928, 929 can operate as a locking system or latchingsystem 905. The relief groove 931 can also contribute to operation ofthe latching system 905. Other suitable latching system arrangements arealso contemplated.

The plug 921 can be configured to transition from the initial positionshown in FIGS. 23A and 23B to the retracted position shown in FIG. 23C.In particular, with reference to FIG. 23B, the connector 302 can form afluid tight seal with the sealing member 941. Interaction between theproximal groove 928 and the detent 951 can be sufficiently strong tomaintain the sealing member 941 in its initial orientation so as to formthe seal with the connector 302. A distal end of the connector 302 maybe spaced from the pad 932 at this point, so as to prevent antisepticfrom entering into the lumen 322 prior to creation of the seal.

Upon further advancement of the connector 302 into the cap 902, theforces on the plug 921 can be sufficient to cause radial compression ofthe support member 934 so as to move the detent 951 to the distal groove929. In some embodiments, the detent 951/groove 929 pairing can maintainthe plug 921 in the retracted position when the medical connector 302 isremoved from the cap 902.

In some embodiments, a cap 1002 can be packaged independently of anothercap when in a pre-use state, such that it may not be part of anassembly. For example, as shown in FIG. 24, in some embodiments, aremovable cover 1086 may be secured to a proximal end of a cap 1002 inany suitable manner, such as, for example, via an adhesive. Preferably,the cover 1086 can be readily removed by a practitioner. The cover 1086may include a graspable tab 1087 to aid in the removal thereof. Theremovable cover 1086 can be formed of any suitable material, such as,for example, an impervious pliable material (e.g., foil, plastic,metallized-surface mylar). Examples of suitable covers are illustratedin U.S. patent application Ser. No. 12/917,336, titled DISINFECTING CAPSAND SYSTEMS AND ASSOCIATED METHODS, filed Nov. 1, 2010.

FIG. 25 illustrates an example of medical connectors 200, 300 for whichcaps disclosed herein may be used. Any suitable variety of medicalconnectors 200, 300 is possible, such as, for example, luer lockconnectors. The connectors 200, 300 are associated with a fluid pathway1100, such as a fluid line 1105 of any suitable variety, which may becoupled with an IV bag 1110 or other suitable fluid delivery system.Commonly, the fluid pathway 1200 can be used to intermittentlyadminister medications to a patient P.

In the illustrated embodiment, the connector 300 of the fluid pathway1100, which communicates fluids with a patient's blood stream, may beselectively disconnected from the connector 200. One or more of theconnectors 200, 300 may be connected to other connectors (not shown),such as a connector associated with a central line. The medicalconnectors 200, 300 may be connected and disconnected at various times,and may remain disconnected for several minutes or hours. Medicalconnector caps disclosed herein can be used to cover and protect thevarious medical connectors 200, 300 while the connectors are separatedfrom one another.

The foregoing disclosure recites various embodiments that include capsthat are configured to disinfect medical connectors. Certain of suchcaps can include a housing that defines a connection interface and thatdefines a chamber in which an antiseptic is retained. Illustrativeexamples of means for sealing a fluid path of a medical connectorinclude the sealing members 141, 190, 441, 541, 641, 741, 841, and 941.Illustrative examples of means for supporting the means for sealing afluid path include the supporting members 134, 176, 434, 534, 634, 734,834, and 934.

It will be understood by those having skill in the art that many changesmay be made to the details of the above-described embodiments withoutdeparting from the underlying principles presented herein. For example,any suitable combination of features of the various embodiments ofassemblies described above is contemplated.

Any methods disclosed herein comprise one or more steps or actions forperforming the described method. The method steps and/or actions may beinterchanged with one another. In other words, unless a specific orderof steps or actions is required for proper operation of the embodiment,the order and/or use of specific steps and/or actions may be modified.

It should be appreciated that in the above description of embodiments,various features are sometimes grouped together in a single embodiment,figure, or description thereof for the purpose of streamlining thedisclosure. This method of disclosure, however, is not to be interpretedas reflecting an intention that any claim require more features thanthose expressly recited in that claim. Rather, as the following claimsreflect, inventive aspects lie in a combination of fewer than allfeatures of any single foregoing disclosed embodiment. Thus, the claimsfollowing this Detailed Description are hereby expressly incorporatedinto this Detailed Description, with each claim standing on its own as aseparate embodiment. This disclosure includes all permutations of theindependent claims with their dependent claims.

References to approximations are made throughout this specification,such as by use of the terms “about” or “approximately.” For each suchreference, it is to be understood that, in some embodiments, the value,feature, or characteristic may be specified without approximation. Forexample, where qualifiers such as “about,” “substantially,” and“generally” are used, these terms include within their scope thequalified words in the absence of their qualifiers. For example, wherethe term “substantially planar” is recited with respect to a feature, itis understood that in further embodiments, the feature can have aprecisely planar orientation.

Recitation in the claims of the term “first” with respect to a featureor element does not necessarily imply the existence of a second oradditional such feature or element. Elements recited inmeans-plus-function format are intended to be construed in accordancewith 35 U.S.C. §112¶6. It will be apparent to those having skill in theart that changes may be made to the details of the above-describedembodiments without departing from the underlying principles of theinvention.

1. A cap configured to disinfect a medical connector, the capcomprising: a housing that defines a connection interface that isconfigured to couple the cap with a medical connector, the housingfurther defining a chamber; an antiseptic within the chamber; a sealingmember within the chamber that is moveable relative to at least aportion of the housing, wherein the sealing member is configured tocontact a portion of a medical connector so as to seal a fluid pathdefined by the medical connector when the cap is coupled to the medicalconnector to thereby prevent antiseptic from entering the fluid path;and a support member coupled with the sealing member, wherein thesupport member is configured to transition from an initial orientationrelative to the connection interface to a retracted orientation relativeto the connection interface, and wherein the support member isconfigured to provide a sufficient amount of resistive force to thesealing member so as to permit the sealing member to seal the fluid pathof a medical connector prior to a complete transition of the supportmember into the retracted orientation.
 2. The cap of claim 1, whereinthe support member comprises a deformable pad that includes at least aportion of the antiseptic therein.
 3. The cap of claim 2, wherein thepad is configured to expel antiseptic once compressed such that theantiseptic can move from one side of the sealing member to another sideof the sealing member.
 4. The cap of claim 2, wherein the pad isresiliently deformable such that the pad is configured to return thesealing member from the retracted orientation to the initial orientationwhen the cap is decoupled from a medical connector.
 5. The cap of claim2, wherein a transverse cross-section through the pad is either round orrectangular in shape.
 6. The cap of claim 1, further comprising a padthat comprises at least a portion of the antiseptic therein.
 7. The capof claim 6, wherein the pad extends about at least a portion of thesupport member when the support member is in the initial orientation. 8.The cap of claim 6, wherein the pad extends about at least a portion ofthe sealing member when the support member is in the retractedorientation.
 9. The cap of claim 6, wherein the pad defines a cavity,wherein at least a portion of the support member is positioned withinthe cavity, and wherein the sealing member is configured to move throughat least a portion of the cavity when a medical connector is coupledwith the cap.
 10. The cap of claim 1, wherein the support member iscompressible, and wherein the support member is uncompressed when it isin the initial orientation and is compressed when it is in the retractedorientation.
 11. The cap of claim 1, wherein the support member isresiliently deformable.
 12. The cap of claim 11, wherein the supportmember comprises one or more of a spring and an elastomeric pad.
 13. Thecap of claim 1, wherein the support member is plastically deformable.14. The cap of claim 13, wherein the support member is configured tocollapse upon application of sufficient force to the sealing member. 15.The cap of claim 14, wherein the support member comprises a collapsiblestructure at an interior of the chamber that is positioned between thesealing member and the housing.
 16. The cap of claim 13, wherein thehousing defines at least a portion of the support member.
 17. The cap ofclaim 16, wherein the support member comprises a region of weakness atwhich the housing is thinner than it is in neighboring regions.
 18. Thecap of claim 1, wherein the support member is translatable from aninitial position to a retracted position, the cap further comprising alocking system that is configured to maintain the support member in theinitial position until a sufficient coupling force with a medicalconnector is achieved, at which point the support member is permitted totranslate to the retracted position.
 19. The cap of claim 18, whereinthe locking system is configured to maintain the support member in theretracted position once the support member has been translated thereto.20. The cap of claim 1, wherein the support member is integrally formedwith the sealing member.
 21. The cap of claim 1, wherein at least aportion of a surface of the sealing member is frustoconical.
 22. The capof claim 1, wherein a surface of the sealing member defines a luer tapersuch that at least a portion of the sealing member is configured to bereceived within a lumen defined by a female luer connector so as to sealagainst an inner surface of the luer connector.
 23. The cap of claim 1,wherein the connection interface projects radiallly inwardly from aninwardly facing surface of the housing, and wherein the cap isconfigured to be coupled with a female medical connector.
 24. The cap ofclaim 1, wherein the connection interface projects radially outwardlyfrom an outwardly facing surface of the housing, and wherein the cap isconfigured to be coupled with a male medical connector.
 25. The cap ofclaim 1, wherein the chamber is sized and dimensioned to receive a maleprotrusion of a medical cap therein.
 26. The cap of claim 25, whereinthe male protrusion of the medical connector defines a lumen, andwherein the sealing member is configured to create a fluid-tight sealwith the male protrusion that is capable of preventing fluid fromentering the lumen.
 27. The cap of claim 1, wherein the supportcomprises a pad and a resilient post, wherein the pad is positionedbetween the sealing member and the post, and wherein the sealing memberand the post are configured to cooperate to compress the pad as the capis coupled to a medical connector so as to force antiseptic from thepad.
 28. The cap of claim 27, wherein the support is less compliant thanthe pad such that the pad is more easily compressed than is the support.29. The cap of claim 1, wherein the housing comprises a sidewall thatdefines at least a portion of the chamber, and wherein at least aportion of the sidewall is tapered so as to be able to form a seal witha male luer.
 30. The cap of claim 1, wherein the support member isconfigured to resist movement of the sealing member such that thesealing member forms a seal with a medical connector before any portionof the support member moves toward the retracted orientation.
 31. Thecap of claim 1, wherein the support member is configured to provide asufficient amount of resistive force to the sealing member so as topermit the sealing member to seal the fluid path of a medical connectorprior to any contact being made between the antiseptic and the medicalconnector.
 32. An assembly configured to disinfect one or more medicalconnectors, the assembly comprising: a first cap that comprises ahousing that defines a first connection interface; and a second cap thatcomprises: a housing that defines a first connection interface; asealing member within the chamber that is moveable relative to thehousing, wherein the sealing member is configured to contact a portionof a medical connector so as to seal a fluid path defined by the medicalconnector when the second cap is coupled to the medical connector tothereby prevent antiseptic from entering the fluid path; and a supportmember coupled with the sealing member, wherein the support member isconfigured to transition from an initial orientation relative to thefirst connection interface of the second cap to a retracted orientationrelative to the first connection interface, and wherein the supportmember is configured to provide a sufficient amount of resistive forceto the sealing member so as to permit the sealing member to seal thefluid path of a medical connector prior to a complete transition of thesupport member into the retracted orientation, wherein, when theassembly is in a pre-use configuration, the first and second caps arecoupled with the assembly via their respective first connectioninterfaces. 33-45. (canceled)
 46. A cap configured to disinfect amedical connector, the cap comprising: a housing that defines aconnection interface that is configured to couple the cap with a medicalconnector, the housing further defining a chamber; an antisepticretained within the chamber; means for sealing a fluid path of a medicalconnector, wherein the means for sealing is configured to contact aportion of a medical connector so as to seal a fluid path defined by themedical connector when the cap is coupled to the medical connector tothereby prevent antiseptic from entering the fluid path; and means forsupporting the means for sealing, wherein the means for supporting isconfigured to permit the means for sealing to create a seal with amedical connector before the antiseptic is moved into contact with themedical connector such that seal can prevent the antiseptic fromentering the fluid path of the medical connector.